Researcher: Müftüoğlu, Meltem
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Müftüoğlu, Meltem
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Publication Metadata only Real time and quantitative assessment of the effects of different ovarian stimulation protocols on the proliferation and cell cycle kinetics of granulosa cells using a new impedence-based system(Elsevier, 2013) N/A; N/A; N/A; N/A; Öktem, Özgür; Müftüoğlu, Meltem; Şenbabaoğlu, Filiz; Urman, Cumhur Bülent; Faculty Member; Faculty Member; PHD Student; Faculty Member; School of Medicine; School of Medicine; Graduate School of Health Sciences; School of Medicine; 102627; N/A; N/A; 12147Publication Metadata only Effect of pharmacologic inhibition of c-Jun N-terminal kinase (JNK) signaling pathway on cell proliferation and cell cycle progression in human granulosa cell tumor(Lippincott Williams and Wilkins, 2013) N/A; N/A; Öktem, Özgür; Müftüoğlu, Meltem; Şenbabaoğlu, Filiz; Urman, Cumhur Bülent; Faculty Member; Faculty Member; PhD Student; Faculty Member; School of Medicine; School of Medicine; Graduate School of Health Sciences; School of Medicine; 102627; 105916; N/A; 12147N/APublication Metadata only Real-time analysis of the growth of human granulosa cells using an impedance-based signal processing system: a new technology for translational research in human reproduction(Oxford University Press (OUP), 2013) N/A; N/A; Öktem, Özgür; Müftüoğlu, Meltem; Şenbabaoğlu, Filiz; Urman, Cumhur Bülent; Faculty Member; Faculty Member; PhD Student; Faculty Member; School of Medicine; School of Medicine; Graduate School of Health Sciences; School of Medicine; 102627; 105916; N/A; 12147N/APublication Metadata only Pharmacologic inhibition of c-jun n-terminal kinase (JNK) signaling pathway inhibits proliferation, blocks cell cycle progression and induces apoptosis of human granulosa cell tumor(Lippincott Williams and Wilkins (LWW), 2013) Taskiran, C.; Ata, B.; Arvas, M.; Urman, Cumhur Bülent; Öktem, Özgür; Müftüoğlu, Meltem; Şenbabaoğlu, Fatih; Faculty Member; Faculty Member; Faculty Member; Master Student; School of Medicine; School of Medicine; School of Medicine; Graduate School of Sciences and Engineering; 12147; 102627; 105916; N/AN/APublication Metadata only Multiple interaction partners for cockayne syndrome proteins: implications for genome and transcriptome maintenance(Elsevier Ireland Ltd, 2013) Aamann, Maria D.; Bohr, Vilhelm A.; Stevnsner, Tinna; N/A; Müftüoğlu, Meltem; Faculty Member; School of Medicine; 105916Cockayne syndrome (CS) is characterized by progressive multisystem degeneration and is classified as a segmental premature aging syndrome. The majority of CS cases are caused by defects in the CS complementation group B (CSB) protein and the rest are mainly caused by defects in the CS complementation group A (CSA) protein. Cells from CS patients are sensitive to UV light and a number of other DNA damaging agents including various types of oxidative stress. The cells also display transcription deficiencies, abnormal apoptotic response to DNA damage, and DNA repair deficiencies. Herein we have critically reviewed the current knowledge about known protein interactions of the CS proteins. The review focuses on the participation of the CSB and CSA proteins in many different protein interactions and complexes, and how these interactions inform us about pathways that are defective in the disease.